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一种新型人细小病毒的分离与鉴定。

Isolation and identification of a novel human parechovirus.

作者信息

Ito Miyabi, Yamashita Teruo, Tsuzuki Hideaki, Takeda Naokazu, Sakae Kenji

机构信息

Department of Microbiology, Aichi Prefectural Institute of Public Health, Nagare 7-6, Tsuji-machi, Kita-ku, Nagoya, Aichi 462-8576, Japan.

Department of Virology II, National Institute of Infectious Disease, Tokyo, Japan.

出版信息

J Gen Virol. 2004 Feb;85(Pt 2):391-398. doi: 10.1099/vir.0.19456-0.

Abstract

A cytopathic agent (A308/99) was isolated using Vero cells from a stool specimen of a 1-year-old patient with transient paralysis. The agent was approximately 28 nm in diameter with a distinct ultrastructure resembling the virus particle of an enterovirus. It could not be neutralized by antisera against human picornaviruses such as human enterovirus, Aichi virus or human parechovirus. The virion contained three capsid proteins with molecular masses of 38, 30.3 and 30 kDa. Determination of the complete nucleotide sequence of A308/99 revealed that the nucleotide and deduced amino acid sequences were closely related to those of human parechoviruses. When 11 regions encoding the structural and non-structural proteins were compared, A308/99 had between 75 and 97 % and 73 and 97 % nucleotide identity with human parechovirus type 1 (HPeV-1) and type 2 (HPeV-2), respectively. The most distinctive divergence was seen in VP1, which had 74.5 % and 73.1 % nucleotide identity with HPeV-1 and HPeV-2, respectively. Viruses related to A308/99 were also isolated from three patients with gastroenteritis, exanthema or respiratory illnesses. A308/99 and these other three isolates had no arginine-glycine-aspartic acid (RGD) motif, which is located near the C terminus of VP1 in HPeV-1 and HPeV-2. A seroepidemiological study revealed that the prevalence of A308/99 antibodies was low (15 %) among infants but became higher with age, reaching more than 80 % by 30 years of age. These observations indicate that A308/99 is genetically close to, but serologically and genetically distinct from, HPeV-1 and HPeV-2 and accordingly can be classified as third serotype of human parechovirus.

摘要

从一名患有短暂性麻痹的1岁患者的粪便标本中,利用非洲绿猴肾细胞(Vero细胞)分离出一种细胞病变因子(A308/99)。该因子直径约28纳米,具有独特的超微结构,类似于肠道病毒的病毒颗粒。它不能被针对人类微小核糖核酸病毒(如人类肠道病毒、爱知病毒或人类副埃可病毒)的抗血清中和。病毒粒子含有三种衣壳蛋白,分子量分别为38、30.3和30 kDa。对A308/99完整核苷酸序列的测定表明,其核苷酸和推导的氨基酸序列与人类副埃可病毒密切相关。当比较编码结构蛋白和非结构蛋白的11个区域时,A308/99与1型人类副埃可病毒(HPeV-1)和2型人类副埃可病毒(HPeV-2)的核苷酸同一性分别为75%至97%和73%至97%。最显著的差异出现在VP1中,它与HPeV-1和HPeV-2的核苷酸同一性分别为74.5%和73.1%。与A308/99相关的病毒也从三名患有肠胃炎、皮疹或呼吸道疾病的患者中分离出来。A308/99和其他三株分离株没有精氨酸-甘氨酸-天冬氨酸(RGD)基序,该基序位于HPeV-1和HPeV-2的VP1 C末端附近。一项血清流行病学研究表明,A308/99抗体在婴儿中的流行率较低(15%),但随年龄增长而升高,到30岁时超过80%。这些观察结果表明,A308/99在基因上与HPeV-1和HPeV-2接近,但在血清学和遗传学上不同,因此可归类为人类副埃可病毒的第三种血清型。

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